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Items: 1 to 20 of 949

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057058inversion1nstd229human GRCh38 chr4: 165,065,528-168,877,636 , GRCh37.p13 chr4: 165,986,680-169,798,787 DDX60L, RNA5SP170, 33 more genes
    nsv7056446inversion1nstd229human GRCh38 chr4: 167,109,272-167,116,847 , GRCh37.p13 chr4: 168,030,423-168,037,998 SPOCK3
    nsv7056217inversion1nstd229human GRCh38 chr4: 166,607,935-172,500,612 , GRCh37.p13 chr4: 167,529,086-173,421,763 DDX60, LOC105377529, 50 more genes
    nsv7055927inversion1nstd229human GRCh38 chr4: 167,014,666-167,018,854 , GRCh37.p13 chr4: 167,935,817-167,940,005 SPOCK3
    nsv7054487inversion1nstd229human GRCh38 chr4: 166,924,254-166,982,894 , GRCh37.p13 chr4: 167,845,405-167,904,045 SPOCK3
    nsv7053547inversion1nstd229human GRCh38 chr4: 166,732,045-166,732,083 , GRCh37.p13 chr4: 167,653,196-167,653,234 SPOCK3
    nsv7051932inversion1nstd229human GRCh38 chr4: 167,035,735-167,035,806 , GRCh37.p13 chr4: 167,956,886-167,956,957 SPOCK3
    nsv7048342inversion1nstd229human GRCh38 chr4: 166,738,106-166,745,806 , GRCh37.p13 chr4: 167,659,257-167,666,957 SPOCK3
    nsv7045110inversion1nstd229human GRCh38 chr4: 166,062,112-167,160,645 , GRCh37.p13 chr4: 166,983,264-168,081,796 TLL1, RNA5SP171, 1 more genes
    nsv7042077inversion1nstd229human GRCh38 chr4: 166,462,061-167,518,554 , GRCh37.p13 chr4: 167,383,213-168,439,705 SPOCK3, RNA5SP171, 1 more genes
    nsv7040771inversion1nstd229human GRCh38 chr4: 166,823,273-166,827,598 , GRCh37.p13 chr4: 167,744,424-167,748,749 SPOCK3
    nsv6756987copy number variation1nstd229human GRCh38 chr4: 167,105,201-167,107,900 , GRCh37.p13 chr4: 168,026,352-168,029,051 SPOCK3
    nsv6756753copy number variation1nstd229human GRCh38 chr4: 166,971,568-167,102,695 , GRCh37.p13 chr4: 167,892,719-168,023,846 SPOCK3
    nsv6756702copy number variation1nstd229human GRCh38 chr4: 166,981,060-166,990,590 , GRCh37.p13 chr4: 167,902,211-167,911,741 SPOCK3
    nsv6756213copy number variation1nstd229human GRCh38 chr4: 167,037,978-167,331,522 , GRCh37.p13 chr4: 167,959,129-168,252,673 SPOCK3
    nsv6756135copy number variation1nstd229human GRCh38 chr4: 167,095,023-167,099,136 , GRCh37.p13 chr4: 168,016,174-168,020,287 SPOCK3
    nsv6756030copy number variation1nstd229human GRCh38 chr4: 166,863,201-166,866,600 , GRCh37.p13 chr4: 167,784,352-167,787,751 SPOCK3
    nsv6755970copy number variation1nstd229human GRCh38 chr4: 167,188,901-167,233,000 , GRCh37.p13 chr4: 168,110,052-168,154,151 SPOCK3
    nsv6755966copy number variation1nstd229human GRCh38 chr4: 166,969,527-166,969,555 , GRCh37.p13 chr4: 167,890,678-167,890,706 SPOCK3
    nsv6755885copy number variation1nstd229human GRCh38 chr4: 167,204,087-167,211,183 , GRCh37.p13 chr4: 168,125,238-168,132,334 SPOCK3
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